Adverse events should be reported.
Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in Google Play or Apple App Store.
Adverse events should also be reported to Ipsen via email at pharmacovigilance.uk-ie@ipsen.com or phone on 01753 627777.
A link to the prescribing information can be found in the header.
Renal Cell Carcinoma
Cabometyx® (cabozantinib) Support Materials
CABOMETYX® is indicated as monotherapy for advanced renal cell carcinoma:
• As first-line treatment of adult patients with intermediate or poor risk
• In adults following prior vascular endothelial growth factor (VEGF)-targeted therapy
CABOMETYX®, in combination with nivolumab, is indicated for the first-line treatment of
advanced renal cell carcinoma in adults.
CABOMETYX® + nivolumab 55.6-month median overall survival in 1st line advanced renal cell carcinoma
Early efficacy with sustained long-term overall survival vs sunitinib: At a median follow-up of 55.6 months (48.1 months minimum), CheckMate 9ER data for CABOMETYX® + nivolumab demonstrate a 10.5-month longer mOS vs sunitinib
CMX-UK-005811 | April 2024